Founded 2016 · Kingdom of Saudi Arabia
Localizing biomanufacturing to secure biologics for Saudi Arabia
Developing top talent and accelerating sector growth in line with Saudi Vision 2030 and the National Biotechnology Strategy.
Why SVAX exists
A chronic gap in local discovery, development and manufacturing capability.
The world faces a significant unmet need for biologics and biosimilars. In the member countries of the Organization of Islamic Cooperation the challenge is sharper still — limited access to therapies built for global markets, and few solutions for local health challenges the global industry overlooks.
As a member of the G20, Saudi Arabia is uniquely positioned to lead. SVAX exists to close that gap — to build sovereign capability across the biologics value chain, and to develop the national talent that will run it.
Prof. Mazen Hassanain · Chief Executive Officer
The value chain
From development to the released vial
SVAX runs development, fill-finish, quality release and registration inside the Kingdom, and works with partners upstream for drug substance. The aim is a chain that closes inside the region rather than one that depends on a factory outside it.
Three businesses
Three businesses, one company
Biotech Business
Advanced research and development in biologics and biosimilars. Proprietary programmes built on licensed IP from regional partners, plus co-development across every stage of the drug lifecycle.
→ 02Manufacturing Business
Development and manufacturing services for biologics — cell line development, process optimization, aseptic fill-finish and packaging, to international regulatory standard.
→ 03Advisory Business
An SFDA-certified CRO supporting local and international companies entering the Saudi market — preclinical studies, regulatory affairs, and biomanufacturing training that builds national capability.
→Infrastructure
One facility in Jeddah, built for commercial scale
SVAX is building a single aseptic fill-finish facility in Jeddah. Build-out runs through 2026, with manufacturing readiness targeted for the first quarter of 2027.
Build-out
Construction and equipment installation at the Jeddah site.
Qualification and licence
Commissioning, cleanroom qualification, and the SFDA site licence.
First production
First commercial batch released to specification.
Jeddah · Under construction
A sterile fill-finish facility, built to international GMP
Isolator-based aseptic filling, automated inspection and grade-controlled cleanrooms. Build-out runs through 2026; commissioning, cleanroom qualification and the SFDA site licence follow, with manufacturing readiness targeted for Q1 2027.
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